Remotely
crmgcpclinical researchdata integritysite monitoringrecruitmentrisk based monitoring
Job Description
📋 Description
- Primary contact for investigative site; connects stakeholders and strengthens AbbVie’s position
- Aligns and trains site staff and investigators on trial goals and patient treatment principles
- Conducts site evaluation, training, monitoring activities with GCP/ICH compliance
- Customizes site engagement strategy using CRM tools to report progress and impact
- Connects protocol and clinical trial requirements to day-to-day execution; supports recruitment and
- Mentors less experienced CRAs and participates in task forces as assigned
🎯 Requirements
- Tertiary qualification in health-related disciplines preferred
- Minimum 1 year clinically related experience; 6 months in clinical research monitoring
- Knowledge of regulatory requirements, ICH/GCP guidelines, and applicable policies
- Strong cross-functional collaboration, planning, and organizational skills
- Proficient in leveraging technology/resources for site-centric support
- Excellent interpersonal, communication, and presentation skills; integrity and collaboration
🎁 Benefits
- AbbVie is an equal opportunity employer
- Comprehensive benefits package; PTO, medical/dental/vision, 401(k)
- Eligibility for short-term incentive programs
- Pay range disclosed in posting; varies by location and grade
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